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Living Alone is Predictive of Non-home Discharge Following Elective Total Hip Arthroplasty: a Matched-pairs Cohort Analysis

Completed
Conditions
Arthropathy of Hip
Perioperative/Postoperative Complications
Interventions
Behavioral: home support, hiving alone
Behavioral: home support, living with others
Registration Number
NCT06462885
Lead Sponsor
University of Virginia
Brief Summary

The goal of this observational study is to assess the effect of living alone on total hip arthroplasty thirty-day outcomes. The main questions it aims to answer are:

Is living alone associated with discharge disposition (home versus non-home)? Is living alone associated with greater incidences of secondary adverse events?

Participants will be sampled from the 2021 American College of Surgeons National Surgical Quality Improvement Program

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
5677
Inclusion Criteria
  • Elective, non-emergent cases
  • Living alone
  • Living with others
Exclusion Criteria
  • Fracture in surgical diagnosis
  • Hospital admission >1 day preoperatively
  • End-stage renal disease (preoperative)
  • Metastatic disease (preoperative)
  • Sepsis (preoperative)
  • Bleeding diathesis (preoperative)
  • American Society of Anesthesiologists Physical Status Classification 5

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Living alonehome support, hiving alone1,624 patients undergoing elective total hip arthroplasty who were living alone at the time of admission.
Living with othershome support, living with others1,624 patients undergoing elective total hip arthroplasty who were living with others at the time of admission.
Primary Outcome Measures
NameTimeMethod
Discharge dispositionThirty days

Home versus non-home

Secondary Outcome Measures
NameTimeMethod
Hospital length of stayThirty days
Wound complicationsThirty days

Superficial surgical site infection (SSI), deep incisional SSI, organ space SSI, and wound dehiscence

Requiring home servicesThirty days
Postoperative deliriumThirty days
Unplanned resource utilizationThirty days

Unplanned readmission and return to the operating room

Functional status at dischargeThirty days

Dependent versus independent

Bleeding eventsThirty days

Requiring transfusion

MortalityThirty days
Systemic complicationsThirty days

Cardiac arrest, myocardial infarction, stroke, reintubation, pneumonia, deep venous thrombosis, pulmonary embolism, bleeding, sepsis, septic shock, and acute kidney injury

Trial Locations

Locations (1)

University of Virginia

🇺🇸

Charlottesville, Virginia, United States

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